Пластиды: органеллы растений, фотосинтез и запасание крахмала.

Plant cell organelles that perform photosynthesis and store starch

A plastid , , is a membrane bound organelle found in the cells of plants, algae, and some other eukaryotic organisms. They are considered to be intracellular endosymbiotic cyanobacteria. Examples of plastids include chloroplasts (used for photosynthesis); chromoplasts (used for synthesis and storage of pigments); leucoplasts (non pigmented plastids some of which can differentiate); and apicoplasts (non photosynthetic plastids of apicomplexa derived from secondary endosymbiosis). A permanent primary endosymbiosis event occurred about 1.5 billion years ago in the Archaeplastida cladeland plants, red algae, green algaeprobably with a cyanobiont, a symbiotic cyanobacteria related to the genus Gloeomargarita. Another primary endosymbiosis event occurred later, between 140 to 90 million years ago, in the photosynthetic plastids Paulinella amoeboids of the cyanobacteria genera Prochlorococcus and Synechococcus, or the "PS clade". Secondary and tertiary endosymbiosis events have also occurred in a wide variety of organisms; and some organisms developed the capacity to sequester ingested plastidsa process known as kleptoplasty. A. F. W. Schimper was the first to name, describe, and provide a clear definition of plastids, which possess a double stranded DNA molecule that long has been thought as circular in shape, like that of the circular chromosome of prokaryotic cellsbut now, perhaps not; (see " a linear shape"). Plastids are sites for manufacturing and storing pigments and other important chemical compounds used by the cells of autotrophic eukaryotes. Some contain biological pigments such as used in photosynthesis or which determine a cell's color. Plastids in organisms that have lost their photosynthetic properties are highly useful for manufacturing molecules like the isoprenoids.

Each plastid creates multiple copies of its own unique genome, or plastome, (from 'plastid genome')which for a chlorophyll plastid (or chloroplast) is equivalent to a 'chloroplast genome', or a 'chloroplast DNA'. The number of genome copies produced per plastid is variable, ranging from 1000 or more in rapidly dividing new cells, encompassing only a few plastids, down to 100 or less in mature cells, encompassing numerous plastids. A plastome typically contains a genome that encodes transfer ribonucleic acids (tRNA)s and ribosomal ribonucleic acids (rRNAs). It also contains proteins involved in photosynthesis and plastid gene transcription and translation. But these proteins represent only a small fraction of the total protein set up necessary to build and maintain any particular type of plastid. Nuclear genes (in the cell nucleus of a plant) encode the vast majority of plastid proteins; and the expression of nuclear and plastid genes is co regulated to coordinate the development and differention of plastids. Many plastids, particularly those responsible for photosynthesis, possess numerous internal membrane layers. Plastid DNA exists as protein DNA complexes associated as localized regions within the plastid's inner envelope membrane; and these complexes are called 'plastid nucleoids'. Unlike the nucleus of a eukaryotic cell, a plastid nucleoid is not surrounded by a nuclear membrane. The region of each nucleoid may contain more than 10 copies of the plastid DNA. Where the proplastid (undifferentiated plastid) contains a single nucleoid region located near the centre of the proplastid, the developing (or differentiating) plastid has many nucleoids localized at the periphery of the plastid and bound to the inner envelope membrane. During the development/ differentiation of proplastids to chloroplastsand when plastids are differentiating from one type to anothernucleoids change in morphology, size, and location within the organelle. The remodelling of plastid nucleoids is believed to occur by modifications to the abundance of and the composition of nucleoid proteins. In normal plant cells long thin protuberances called stromules sometimes formextending from the plastid body into the cell cytosol while interconnecting several plastids. Proteins and smaller molecules can move around and through the stromules. Comparatively, in the laboratory, most cultured cellswhich are large compared to normal plant cellsproduce very long and abundant stromules that extend to the cell periphery. In 2014, evidence was found of the possible loss of plastid genome in Rafflesia lagascae, a non photosynthetic parasitic flowering plant, and in Polytomella, a genus of non photosynthetic green algae. Extensive searches for plastid genes in both taxons yielded no results, but concluding that their plastomes are entirely missing is still disputed. Some scientists argue that plastid genome loss is unlikely since even these non photosynthetic plastids contain genes necessary to complete various biosynthetic pathways including heme biosynthesis. Even with any loss of plastid genome in Rafflesiaceae, the plastids still occur there as "shells" without DNA content, which is reminiscent of hydrogenosomes in various organisms.

In reproducing, most plants inherit their plastids from only one parent. In general, angiosperms inherit plastids from the female gamete, where many gymnosperms inherit plastids from the male pollen. Algae also inherit plastids from just one parent. Thus the plastid DNA of the other parent is completely lost. In normal intraspecific crossingsresulting in normal hybrids of one speciesthe inheriting of plastid DNA appears to be strictly uniparental; i. e., from the female. In interspecific hybridisations, however, the inheriting is apparently more erratic. Although plastids are inherited mainly from the female in interspecific hybridisations, there are many reports of hybrids of flowering plants producing plastids from the male. Approximately 20% of angiosperms, including alfalfa (Medicago sativa), normally show biparental inheriting of plastids.

The plastid DNA of maize seedlings is subjected to increasing damage as the seedlings develop. The DNA damage is due to oxidative environments created by photo oxidative reactions and photosynthetic/ respiratory electron transfer. Some DNA molecules are repaired but DNA with unrepaired damage is apparently degraded to non functional fragments. DNA repair proteins are encoded by the cell's nuclear genome and then translocated to plastids where they maintain genome stability/ integrity by repairing the plastid's DNA. For example, in chloroplasts of the moss Physcomitrella patens, a protein employed in DNA mismatch repair (Msh1) interacts with proteins employed in recombinational repair (RecA and RecG) to maintain plastid genome stability.

Plastids are thought to be descended from endosymbiotic cyanobacteria. The primary endosymbiotic event of the Archaeplastida is hypothesized to have occurred around 1.5 billion years ago and enabled eukaryotes to carry out oxygenic photosynthesis. Three evolutionary lineages in the Archaeplastida have since emerged in which the plastids are named differently: chloroplasts in green algae and/or plants, rhodoplasts in red algae, and muroplasts in the glaucophytes. The plastids differ both in their pigmentation and in their ultrastructure. For example, chloroplasts in plants and green algae have lost all phycobilisomes, the light harvesting complexes found in cyanobacteria, red algae and glaucophytes, but instead contain stroma and grana thylakoids. The glaucocystophycean plastid—in contrast to chloroplasts and rhodoplasts—is still surrounded by the remains of the cyanobacterial cell wall. All these primary plastids are surrounded by two membranes. The plastid of photosynthetic Paulinella species is often referred to as the 'cyanelle' or chromatophore, and had a much more recent endosymbiotic event about 90–140 million years ago; it is the only known primary endosymbiosis event of cyanobacteria outside of the Archaeplastida. When a eukaryote engulfs a red or a green alga and retains the algal plastid, that plastid is typically surrounded by more than two membranes. In some cases these plastids may be reduced in their metabolic and/or photosynthetic capacity. Algae with complex plastids derived by secondary endosymbiosis of a red alga include the heterokonts, haptophytes, cryptomonads, and most dinoflagellates (= rhodoplasts). Those that endosymbiosed a green alga include the euglenids and chlorarachniophytes (= chloroplasts). The Apicomplexa, a phylum of obligate parasitic alveolates including the causative agents of malaria (Plasmodium spp. ), toxoplasmosis (Toxoplasma gondii), and many other human or animal diseases also harbor a complex plastid (although this organelle has been lost in some apicomplexans, such as Cryptosporidium parvum, which causes cryptosporidiosis). The 'apicoplast' is no longer capable of photosynthesis, but is an essential organelle, and a promising target for antiparasitic drug development. Some dinoflagellates and sea slugs, in particular of the genus Elysia, take up algae as food and keep the plastid of the digested alga to profit from the photosynthesis; after a while, the plastids are also digested. This process is known as kleptoplasty, from the Greek, kleptes (κλέπτης), thief.

In 1977 J. M Whatley proposed a plastid development cycle which said that plastid development is not always unidirectional but is instead a complicated cyclic process. Proplastids are the precursor of the more differentiated forms of plastids, as shown in the diagram to the right.